Cargando…
Serotonergic Innervations of the Orbitofrontal and Medial-prefrontal Cortices are Differentially Involved in Visual Discrimination and Reversal Learning in Rats
Cross-species studies have identified an evolutionarily conserved role for serotonin in flexible behavior including reversal learning. The aim of the current study was to investigate the contribution of serotonin within the orbitofrontal cortex (OFC) and medial prefrontal cortex (mPFC) to visual dis...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7906782/ https://www.ncbi.nlm.nih.gov/pubmed/33043981 http://dx.doi.org/10.1093/cercor/bhaa277 |
_version_ | 1783655362696577024 |
---|---|
author | Alsiö, Johan Lehmann, Olivia McKenzie, Colin Theobald, David E Searle, Lydia Xia, Jing Dalley, Jeffrey W Robbins, Trevor W |
author_facet | Alsiö, Johan Lehmann, Olivia McKenzie, Colin Theobald, David E Searle, Lydia Xia, Jing Dalley, Jeffrey W Robbins, Trevor W |
author_sort | Alsiö, Johan |
collection | PubMed |
description | Cross-species studies have identified an evolutionarily conserved role for serotonin in flexible behavior including reversal learning. The aim of the current study was to investigate the contribution of serotonin within the orbitofrontal cortex (OFC) and medial prefrontal cortex (mPFC) to visual discrimination and reversal learning. Male Lister Hooded rats were trained to discriminate between a rewarded (A+) and a nonrewarded (B−) visual stimulus to receive sucrose rewards in touchscreen operant chambers. Serotonin was depleted using surgical infusions of 5,7-dihydroxytryptamine (5,7-DHT), either globally by intracebroventricular (i.c.v.) infusions or locally by microinfusions into the OFC or mPFC. Rats that received i.c.v. infusions of 5,7-DHT before initial training were significantly impaired during both visual discrimination and subsequent reversal learning during which the stimulus–reward contingencies were changed (A− vs. B+). Local serotonin depletion from the OFC impaired reversal learning without affecting initial discrimination. After mPFC depletion, rats were unimpaired during reversal learning but slower to respond at the stimuli during all the stages; the mPFC group was also slower to learn during discrimination than the OFC group. These findings extend our understanding of serotonin in cognitive flexibility by revealing differential effects within two subregions of the prefrontal cortex in visual discrimination and reversal learning. |
format | Online Article Text |
id | pubmed-7906782 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-79067822021-03-02 Serotonergic Innervations of the Orbitofrontal and Medial-prefrontal Cortices are Differentially Involved in Visual Discrimination and Reversal Learning in Rats Alsiö, Johan Lehmann, Olivia McKenzie, Colin Theobald, David E Searle, Lydia Xia, Jing Dalley, Jeffrey W Robbins, Trevor W Cereb Cortex Original Article Cross-species studies have identified an evolutionarily conserved role for serotonin in flexible behavior including reversal learning. The aim of the current study was to investigate the contribution of serotonin within the orbitofrontal cortex (OFC) and medial prefrontal cortex (mPFC) to visual discrimination and reversal learning. Male Lister Hooded rats were trained to discriminate between a rewarded (A+) and a nonrewarded (B−) visual stimulus to receive sucrose rewards in touchscreen operant chambers. Serotonin was depleted using surgical infusions of 5,7-dihydroxytryptamine (5,7-DHT), either globally by intracebroventricular (i.c.v.) infusions or locally by microinfusions into the OFC or mPFC. Rats that received i.c.v. infusions of 5,7-DHT before initial training were significantly impaired during both visual discrimination and subsequent reversal learning during which the stimulus–reward contingencies were changed (A− vs. B+). Local serotonin depletion from the OFC impaired reversal learning without affecting initial discrimination. After mPFC depletion, rats were unimpaired during reversal learning but slower to respond at the stimuli during all the stages; the mPFC group was also slower to learn during discrimination than the OFC group. These findings extend our understanding of serotonin in cognitive flexibility by revealing differential effects within two subregions of the prefrontal cortex in visual discrimination and reversal learning. Oxford University Press 2020-10-12 /pmc/articles/PMC7906782/ /pubmed/33043981 http://dx.doi.org/10.1093/cercor/bhaa277 Text en © The Author(s) 2020. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Alsiö, Johan Lehmann, Olivia McKenzie, Colin Theobald, David E Searle, Lydia Xia, Jing Dalley, Jeffrey W Robbins, Trevor W Serotonergic Innervations of the Orbitofrontal and Medial-prefrontal Cortices are Differentially Involved in Visual Discrimination and Reversal Learning in Rats |
title | Serotonergic Innervations of the Orbitofrontal and Medial-prefrontal Cortices are Differentially Involved in Visual Discrimination and Reversal Learning in Rats |
title_full | Serotonergic Innervations of the Orbitofrontal and Medial-prefrontal Cortices are Differentially Involved in Visual Discrimination and Reversal Learning in Rats |
title_fullStr | Serotonergic Innervations of the Orbitofrontal and Medial-prefrontal Cortices are Differentially Involved in Visual Discrimination and Reversal Learning in Rats |
title_full_unstemmed | Serotonergic Innervations of the Orbitofrontal and Medial-prefrontal Cortices are Differentially Involved in Visual Discrimination and Reversal Learning in Rats |
title_short | Serotonergic Innervations of the Orbitofrontal and Medial-prefrontal Cortices are Differentially Involved in Visual Discrimination and Reversal Learning in Rats |
title_sort | serotonergic innervations of the orbitofrontal and medial-prefrontal cortices are differentially involved in visual discrimination and reversal learning in rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7906782/ https://www.ncbi.nlm.nih.gov/pubmed/33043981 http://dx.doi.org/10.1093/cercor/bhaa277 |
work_keys_str_mv | AT alsiojohan serotonergicinnervationsoftheorbitofrontalandmedialprefrontalcorticesaredifferentiallyinvolvedinvisualdiscriminationandreversallearninginrats AT lehmannolivia serotonergicinnervationsoftheorbitofrontalandmedialprefrontalcorticesaredifferentiallyinvolvedinvisualdiscriminationandreversallearninginrats AT mckenziecolin serotonergicinnervationsoftheorbitofrontalandmedialprefrontalcorticesaredifferentiallyinvolvedinvisualdiscriminationandreversallearninginrats AT theobalddavide serotonergicinnervationsoftheorbitofrontalandmedialprefrontalcorticesaredifferentiallyinvolvedinvisualdiscriminationandreversallearninginrats AT searlelydia serotonergicinnervationsoftheorbitofrontalandmedialprefrontalcorticesaredifferentiallyinvolvedinvisualdiscriminationandreversallearninginrats AT xiajing serotonergicinnervationsoftheorbitofrontalandmedialprefrontalcorticesaredifferentiallyinvolvedinvisualdiscriminationandreversallearninginrats AT dalleyjeffreyw serotonergicinnervationsoftheorbitofrontalandmedialprefrontalcorticesaredifferentiallyinvolvedinvisualdiscriminationandreversallearninginrats AT robbinstrevorw serotonergicinnervationsoftheorbitofrontalandmedialprefrontalcorticesaredifferentiallyinvolvedinvisualdiscriminationandreversallearninginrats |